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American Journal of Human Genetics|January 1, 1993
Linkage analysis of "necessary" disease loci versus "susceptibility" lociD A GreenbergAmerican Journal of Human Genetics|January 1, 1993
Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutationR P Ketterling, E Vielhaber, C D Bottema, et al.American Journal of Human Genetics|January 1, 1993
Constitutional 1p36 deletion in a child with neuroblastomaJ A Biegel, P S White, H N Marshall, et al.American Journal of Human Genetics|January 1, 1993
Uniparental disomy for chromosome 16 in humansD K Kalousek, S Langlois, I Barrett, et al.American Journal of Human Genetics|February 1, 1993
Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysisL Varesco, V Gismondi, R James, et al.American Journal of Human Genetics|March 1, 1977
Electrophoretic abnormalities of lysosomal enzymes in mucolipidosis fibroblast linesM J Champion, T B ShowsAmerican Journal of Human Genetics|May 10, 2011
Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndromeXose S Puente, Victor Quesada, Fernando G Osorio, et al.American Journal of Human Genetics|May 10, 2011
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairmentMargit Schraders, Stefan A Haas, Nicole J D Weegerink, et al.American Journal of Human Genetics|March 1, 1997
Familiality of physical and metabolic characteristics that predict the development of non-insulin-dependent diabetes mellitus in Pima IndiansH Sakul, R Pratley, L Cardon, et al.American Journal of Human Genetics|February 1, 1997
Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3qM K Wirtz, J R Samples, P L Kramer, et al.Pageof 979